翻訳と辞書 ・ 1,1-Diethoxyethane ・ 1,1-Difluoroethane ・ 1,1-Difluoroethylene ・ 1,1-Ethanedithiol ・ 1,2,3 Soleils ・ 1,2,3,4,6-Pentagalloyl glucose ・ 1,2,3,4-Tetraphenylnaphthalene ・ 1,2,3,5-Tetrahydroxybenzene ・ 1,2,3-Triazole ・ 1,2,3-Tribromopropane ・ 1,2,3-Trichloropropane ・ 1,2,3-Trimethylbenzene ・ 1,2,3-Trinitrobenzene ・ 1,2,4-Butanetriol ・ 1,2,4-Butanetriol trinitrate ・ 1,2,4-Triazole ・ 1,2,4-Trichlorobenzene ・ 1,2,4-Trihydroxyanthraquinone ・ 1,2,4-Trimethylbenzene ・ 1,2,4-Trioxane ・ 1,2,6-Trigalloyl glucose ・ 1,2-alpha-L-fucosidase ・ 1,2-alpha-mannosidase ・ 1,2-Benzenedithiol ・ 1,2-Benzoquinone ・ 1,2-Bis(dicyanomethylene)squarate ・ 1,2-Bis(diisopropylphosphino)ethane ・ 1,2-Bis(dimethylarsino)benzene ・ 1,2-Bis(dimethylphosphino)ethane ・ 1,2-Bis(diphenylphosphino)ethane
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1,2,4-Triazole : ウィキペディア英語版 | 1,2,4-Triazole
| Section2 = | Section7 = | Section8 = }} 1,2,4-Triazole is one of a pair of isomeric chemical compounds with molecular formula C2H3N3, called triazoles, which have a five-membered ring of two carbon atoms and three nitrogen atoms. 1,2,4-Triazole is a basic aromatic heterocycle. 1,2,4-Triazole derivatives find use in a wide variety of applications, most notably as antifungals such as fluconazole and itraconazole. 1,2,4-Triazoles can be prepared using the Einhorn–Brunner reaction or the Pellizzari reaction. The ring structure appears in certain N-heterocyclic carbenes. == See also ==
* Used in the preparation of Rizatriptan.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「1,2,4-Triazole」の詳細全文を読む
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